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揭示ALK靶向治疗在非小细胞肺癌中的潜力:全面见解与未来方向

Unraveling the Potential of ALK-Targeted Therapies in Non-Small Cell Lung Cancer: Comprehensive Insights and Future Directions.

作者信息

Parvaresh Hannaneh, Roozitalab Ghazaal, Golandam Fatemeh, Behzadi Payam, Jabbarzadeh Kaboli Parham

机构信息

Department of Biology, Faculty of Science, Ferdowsi University of Mashhad, Mashhad 9177948974, Iran.

Division of Cancer Discovery Network, Dr. Parham Academy, Taichung 40602, Taiwan.

出版信息

Biomedicines. 2024 Jan 27;12(2):297. doi: 10.3390/biomedicines12020297.

Abstract

This review comprehensively explores the intricate landscape of anaplastic lymphoma kinase (ALK), focusing specifically on its pivotal role in non-small cell lung cancer (NSCLC). Tracing ALK's discovery, from its fusion with nucleolar phosphoprotein (NPM)-1 in anaplastic large cell non-Hodgkin's lymphoma (ALCL) in 1994, the review elucidates the subsequent impact of ALK gene alterations in various malignancies, including inflammatory myofibroblastoma and NSCLC. Approximately 3-5% of NSCLC patients exhibit complex ALK rearrangements, leading to the approval of six ALK-tyrosine kinase inhibitors (TKIs) by 2022, revolutionizing the treatment landscape for advanced metastatic ALK + NSCLC. Notably, second-generation TKIs such as alectinib, ceritinib, and brigatinib have emerged to address resistance issues initially associated with the pioneer ALK-TKI, crizotinib. To ensure comprehensiveness, we extensively reviewed clinical trials on ALK inhibitors for NSCLC by 2023. Additionally, we systematically searched PubMed, prioritizing studies where the terms "ALK" AND "non-small cell lung cancer" AND/OR "NSCLC" featured prominently in the titles. This approach aimed to encompass a spectrum of relevant research studies, ensuring our review incorporates the latest and most pertinent information on innovative and alternative therapeutics for ALK + NSCLC. Beyond exploring the intricate details of ALK structure and signaling, the review explores the convergence of ALK-targeted therapy and immunotherapy, investigating the potential of immune checkpoint inhibitors in ALK-altered NSCLC tumors. Despite encouraging preclinical data, challenges observed in trials assessing combinations such as nivolumab-crizotinib, mainly due to severe hepatic toxicity, emphasize the necessity for cautious exploration of these novel approaches. Additionally, the review explores innovative directions such as ALK molecular diagnostics, ALK vaccines, and biosensors, shedding light on their promising potential within ALK-driven cancers. This comprehensive analysis covers molecular mechanisms, therapeutic strategies, and immune interactions associated with ALK-rearranged NSCLC. As a pivotal resource, the review guides future research and therapeutic interventions in ALK-targeted therapy for NSCLC.

摘要

本综述全面探讨了间变性淋巴瘤激酶(ALK)的复杂情况,特别关注其在非小细胞肺癌(NSCLC)中的关键作用。回顾ALK的发现历程,从1994年它在间变性大细胞非霍奇金淋巴瘤(ALCL)中与核仁磷蛋白(NPM)-1融合开始,该综述阐明了ALK基因改变在各种恶性肿瘤中的后续影响,包括炎性肌成纤维细胞瘤和NSCLC。大约3%-5%的NSCLC患者表现出复杂的ALK重排,到2022年六种ALK酪氨酸激酶抑制剂(TKIs)获批,彻底改变了晚期转移性ALK+NSCLC的治疗格局。值得注意的是,第二代TKIs如阿来替尼、色瑞替尼和布加替尼已出现,以解决最初与第一代ALK-TKI克唑替尼相关的耐药问题。为确保全面性,我们广泛回顾了截至2023年针对NSCLC的ALK抑制剂的临床试验。此外,我们系统检索了PubMed,优先选择标题中显著包含“ALK”和“非小细胞肺癌”及/或“NSCLC”的研究。这种方法旨在涵盖一系列相关研究,确保我们的综述纳入有关ALK+NSCLC创新和替代疗法的最新及最相关信息。除了探索ALK结构和信号传导的复杂细节外,该综述还探讨了ALK靶向治疗与免疫治疗的融合,研究免疫检查点抑制剂在ALK改变的NSCLC肿瘤中的潜力。尽管临床前数据令人鼓舞,但在评估如纳武利尤单抗-克唑替尼联合用药的试验中观察到的挑战,主要是由于严重的肝毒性,强调了谨慎探索这些新方法的必要性。此外,该综述还探讨了ALK分子诊断、ALK疫苗和生物传感器等创新方向,揭示了它们在ALK驱动的癌症中的潜在前景。这一全面分析涵盖了与ALK重排NSCLC相关的分子机制、治疗策略和免疫相互作用。作为一个关键资源,该综述为NSCLC的ALK靶向治疗的未来研究和治疗干预提供了指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4fc/10887432/07ac0e3e13c7/biomedicines-12-00297-g001.jpg

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